Ce Certification

What are the requirements for automotive parts and components to be allowed in the European market?

In Europe, the quality of your products is often measured by meeting specific requirements. Failure to fulfill or fail to meet these requirements will or will disrupt your attempts to find buyers in the European market.

1.  Requirements to meet

Type approval – Compliance with technical standards for motor vehicles

All Vehicle Type Approval  (WVTA) is a certificate for various types and types of motor vehicles. EU legislation has introduced strict conditions for the harmonization of technical, safety and environmental standards among EU Member States (vehicles) and for agricultural and forestry tractors.

This type of approval or certification is valid in all EU Member States and is necessary when you wish to sell your products in the EU. Many automotive components have not been approved until final assembly. In these cases, it is not necessary to certify individual components; however, these components will have to comply with the type-approval requirements.

In 2017 the testing process will change. In addition to the current laboratory emissions and fuel consumption tests (  New European Driving Cycle  ), a  Real Driving Emission  (RDE) test will be performed. Europe is also   contributing to the development of a new global testing system called the World Wide Harmonized Light Vehicle Testing Procedure (WLTP).


  • The Original Equipment Manufacturer and / or the approval authority determine the specific requirements that you must fulfill. These requirements vary widely per product and per market. This means that you may need to meet different requirements for different buyers and countries you export. Check the  specific type approval requirements of the receiver or approval authority for the parts you produce  .
  • An important requirement of the type approval certificate is the Production Eligibility (COP). COP, in conformity with the specification, performance and marking requirements in the product type validation legislation, refers to the ability to be produced in series which does not require another test. Make sure you have a suitable quality management system in place (see also dan Partner buyer requirements management section).

CE marking

Electronic equipment must be CE marked for marketing in the EU. The CE marking indicates that a product is assessed before it is placed on the market and meets EU safety, health and environmental protection requirements. The CE marking is sometimes also considered a means of conformity to the type-approval requirements; For example, electronic components requiring type approval and also electromagnetic compatibility (EMC) or CE marking for low-voltage equipment.


  •  Learn more about the type approval in the EU Export Help Desk  .
  •  Learn more about the CE marking of electrical equipment in the EU Export Help Desk  .
  •  Follow step-by-step guidance in CE marking  .
  • If you are an electronics or electrical engineering manufacturer in the automotive industry   take a look at our work on these issues .


To prevent environmental damage, the EU has restricted the use of certain chemicals in certain Regulations and Directives.


  • In most cases, it is your EU buyer who is responsible for complying with the legislation on chemicals. Share information with your buyer regarding the substances used in your product, thus proving that it complies with all relevant legislation.
  • Ask your buyer about the chemicals policies and their expectations. Sometimes these directions are called ”black / gray“ lists. Does it provide a list of items you cannot use or would you like to receive information about the substances you use in a certain way? If you don’t yet know your buyer, try looking at a chemicals policy for a car brand. For example, ‘calling Volvo REACH.
Ce Belgeleri

Why CE Marking?

The European CE marking regulation has been mainly set up to:

  • Harmonize all varying national regulations for consumer and industrial products in European Member States, so that the Single Market is encouraged;
  • Bring about cost savings for producers;
  • Enhance the safety of products;
  • Supply public bodies with a uniform procedure that can be checked.In the past, product requirements and test procedures in Europe were set by the individual Member States of the European Union. This meant that, for example, companies that wanted to sell their products on the European market sometimes had to deal with more than ten different technical requirements or procedures for just one product. The existence of all the different national legislation was contrary to the aim of the European Union in realizing one Single Market, in which there would be a free circulation of goods (as well as a free circulation of persons, services and capital).

CE marking Directives or ‘New Approach’ Directives

All the different product requirements brought many costs for the producers. With the help of the CE marking Directives or ‘New Approach’ Directives, the measures have been optimized by setting up European (European-wide) requirements, the harmonization of national legislation and directives, standards and mutual recognition of the technical standards, tests methods (compliance tests) and test laboratories, so that producers no longer need to adapt their products to the different markets.

In European countries, security and safety

During the process of harmonization the safety level of all products was attuned and raised. In most European countries, safety and health had already been the subject of directives for many years but the safety level was not always satisfactory.

With the help of the conformity assessment procedures, the authorities can ascertain that the products that are placed on the market comply with the requirements as stated in the regulations of the directives. The CE marking is consequently largely for the benefit of the authorities. However, safe products are also necessary for the end user in the work or consumer environment.

CE Certificate of Lighting

EGETEST CENTER LED / Lighting Luminaires CE Certificate / Marking works with qualified test laboratory.

EMC Tests for Lighting

LED / Lighting Fixtures must comply with the Low Voltage Directive and the Electromagnetic Compatibility Regulation.

LED / Lighting Luminaires must be subjected to LVD testing and reporting according to EN 60598-1 and related EN 60598-2-XX standard product specifications in accordance with the Low Voltage Directive .

EN 60598 Standard LED / is the standard series used in the certification process of lighting fixtures. It is used with a second party standard. This second party standard is determined by the purpose of the luminaire (eg EN 60598-2-5: Projectors) In general, the EN 60598 Standard series is as follows:

Standards and directives

  • TS EN 60598-1 Lighting fixtures – Part 1: General rules and tests
  • TS 8698 EN 60598-2-1 Lighting fixtures – Part 2: Special rules – Part one: General purpose, fixed
  • TS EN 60598-2-2 Lighting fixtures – Part 2: Particular requirements Part 2: Recessed fittings
  • TS 8700 EN 60598-2-3 Lighting fixtures – Part 2-3: Specific features – For road and street lighting
  • TS 8701 EN 60598-2-4 Lighting fixtures-Part 2: Special rules – Part 4: General purpose, portable
  • Lighting fixtures – Part 2: Special rules – Part 5: Projectors.


This standard covers the general characteristics of LED / Lighting fixtures operating with supply voltages up to 1000 V, combined with electrical light sources.

Another issue that should be considered is the Electromagnetic Compatibility Regulation.

TS EN 55015 Limit values ​​and measurement methods of radio distortion characteristics of electrical lighting and similar devices,

TS EN 61547 Devices used for general lighting purposes – Emu Immunity Rules

It must comply with its standards. The Low Voltage Directive for Lighting Products alone is not sufficient, but they must also comply with the Electromagnetic Compatibility Regulation.

LED / Lighting Fixtures Contact us for LVD and EMC Tests , we are in charge with our Test Laboratory.


CE Certificate Approval Process and Cost

Compliance with the standards defined by CE marking

CE marking, which indicates that the product will not harm human health and nature in case it is used in accordance with its production purpose, also shows that it will work in harmony with other products, equipment and devices used in the same environment. As the precondition for the sale by the European Union, it is demanded to meet the standards defined by the CE marking and the European Union harmonization process is continuing These standards, which are defined by CE certificate, are closely related to manufacturing companies in our country. Although it is considered that the companies doing research about what is required to obtain CE certificate are only enterprises that aim to export to the European Union, it is preferred that the products have CE marking even in private or public tenders in our country.

Cost of obtaining CE certificate from the design stage of the companies

The product that is intended to be placed on the market in vital issues such as human health and nature-friendly use, failure to meet the CE marking standard, which sets the qualitatively acceptable minimum level of safety and compliance; it means that the product is not safe for use and therefore is not allowed to be sold. Instead of developing strategies according to the results of the applications to be made after production in the calculations related to the cost of obtaining CE certificate from the design stage of the companies,It would be best to produce their plans from the outset to meet the requirements. The cost of obtaining the CE certificate in case of exhibiting the attitude according to the result of the application and if the expected approval is not obtained, The costs of the product’s will be much higher, as it requires planning from scratch, from design to production.

CE certification and legislation

In addition to prevention of time loss, our company provides consultancy services in order to get rid of high costs caused by starting the production process from zero. In addition to providing guidance on what is required to obtain CE certification and legislation, it also conducts laboratory tests to determine the characteristics of products such as LVD and EMC. Our expert team will inform you about all processes from the first stage of the application,It allows you to have information about the progress of the approval process by sharing the results of the scientific tests in the laboratory and the results of the required tests simultaneously with you.

For contact and detailed information

When you work with Ege Test Center expert teams, CE Certificate Approval Process and Cost. For detailed information and communication, you can send an e-mail to or fill in the form at and contact us.

CE Certificate for product

Harmonization of your Export Products to CE Standards

CE standardization, which is one of the basic obligations to be met in exports to the European Union; From elevator to toy, from construction materials to low-voltage appliances, from medical supplies to pressurized containers. The inclusion of commercial products, all of which have a wide range of different uses, and which have a wide range of qualifications, depends on the fact that the product meets CE standards, which is the minimum acceptable safety and compliance level.

How to get CE certificate?

The CE marking protocols may appear complex to inexperienced business owners, so the European Standards Committee on Standardization is defined briefly by CEN. Our firm, which eliminates such confusion in the process of applying CE certificate , provides consultancy and guidance on the execution of the application process in a way that will be completed in favor of the manufacturer in accordance with the legal regulations. Experienced and strict implementation of regulations, CE certificate applicationThanks to our team of experts who will ensure that the process is completed in minimum time and without any problems, getting a CE certificate for commercial enterprises becomes a simple job. Our engineering team informs you after completing the preliminary work on all necessary documents and works in a coordinated manner and advises you on how to eliminate deficiencies if needed. The technical file, which includes the studies related to all scientific research and legislation, has been approved by CEN, in other words, your application is made in such a way that you can obtain CE certificate by our organization which has completed its international accreditation.

Application Process for CE Certificate

In addition to the official documents containing the information on the legal status of the commercial enterprise that applies, as well as the signature file of the authorized or representative persons, the application file also contains the text of the agreement between the manufacturer and the firms that make the application. We help you in all matters such as creating records related to documents, preparing system documents, conducting required tests and investigations about products (LVD test, EMC test, etc.) in laboratory environment and conducting certification tests and we enable you to get CE approval without any problem. For all your inquiries about CE marking protocols and applications, just contact us.

Why the CE mark inside?

Thanks to the knowledge and experience of the Egetest Center expert teams for CE Marking, you will be able to sell your product to the European market without any problem. For detailed information and communication, you can mail to or by entering the and You can fill form.

Ce Belgeleri

CE Certification for Machines

As a company, we provide full compatibility within the scope of the directives required for CE Marking in our machines, with no expert staff and technical infrastructure.

For your machines;

2006/42 / EC Machinery Safety Regulation and 2014/35 / EU Low Voltage Directive

  • EN 60204-1 Safety in machines – Electrical equipment of machines – part 1: General rules
  • EN 12100: 10 Safety in machinery – General principles for design – Risk assessment and risk reduction
  • 2006/42 / EC APPENDIX I Review of basic health and safety requirements

Ce Certification

Within the scope of the 2014/35 / EU Electromagnetic Compatibility Directive

EN 61000-6-1 Electromagnetic compatibility (EMU); Section 6-1: General standards-Settlement units, immunity standard for commercial and light industrial environments

  • EN 61000-6-3 Electromagnetic compatibility (emu) – Part 6-3: General standards – Emissions standard for residential, commercial and light industrial environments
  • EN 61000-6-2 Electromagnetic compatibility (EMU) – Part 6-2: General standards – Immunity to industrial environments
  • EN 61000-6-4 Electromagnetic compatibility (emu) – Part 6-4: General standards Flow standard for industrial environments

Technical File Preparation

Preparation of AT Declaration of Conformity

All these tests, inspections and reports will be made by EGE TEST CENTER for our manufacturers with expert engineer staff. We provide full compatibility for your machines with our extensive testing facility, and we do not leave any point in certification.
For our machinery manufacturers, we are able to carry out our tests at the manufacturer’s facilities.

For contact and detailed information

You can send an e-mail to or contact us at and fill out the form.

CE Certificate Acquisition Process

With the expression of expert teams CE Certificate Acquisition Process

The companies that want to get CE Certificate should prepare technical files about the product they want to do first. The technical file that forms the basis of the CE Certificate tender process is required for all products that fall into the risky or risk-free category.

Companies that want to use CE marking must keep the technical file they prepared for the product throughout production. If a functional change is made to the product, the technical file must be refreshed. However, under all other conditions, the technical file must be stored for CE mark validity.

What information should be included in the technical file?

The technical file should contain the basic and technical information about the product to which the CE marking is to be received, as well as the information about the company. The information that should be included in the technical file is as follows:

  • Basic information about the company
  • Label or plate bearing the technical data of the product
  • What the product is used for
  • List of national and international standards used in the production of the product
  • Reports of these tests if you have the test made for the product
  • CE Declaration of Conformity
  • If the manufacturers of the electrical, hydraulic and pneumatic components of the product have been tested and approved by their code numbers and specifications and a competent body,certification about this,
  • Current operating instructions for the product
  • If the product’s supply list and supply products are covered by CE, certificates and test reports of these products
  • Detailed descriptions of how the product is installed, how it works and how the product is maintained.

If there is a deficiency in the technical file

The missing or defective information in the technical dossier will delay the process of obtaining the CE certificate, For this reason, companies must be careful when preparing technical files. It may also be necessary to pass tests such as LVC, EMI and EMC according to the category of the products to which CE certificate is requested. In this case, the technical file should include other tests and reports that should be used in electrical, electronic and telecommunication equipment.


CE Certificate

Incorrect CE Marking and manufacturer responsibility

CE Marking is mandatory for a wide variety of products including all electrical / electronic devices, allowing manufacturers to import and export their products freely within the European Union, with common product design and manufacturing requirements defined within EU Directives. 

By placing the mandatory conformity mark on a product, manufacturers (or if outside of the EU, the importer or authorised representative) are providing a clear indication that it meets all the relevant requirements and should therefore enjoy free movement between all 28 Member states.

Problems with the CE Mark

In recent years, however, Europe has seen an increasing number of goods incorrectly marked with the CE Mark flooding the market from foreign countries. The reasons for this have been three-fold:

  • Firstly, there has been much confusion around the CE Mark itself with similar marks from China often confusing consumers and being mistaken for the genuine CE Mark.
  • Secondly, the CE Mark has been illegitimately placed on products which do not require the Mark, giving consumers the false impression that the product is one of quality.
  • Thirdly, the CE Mark does not represent a product having undergone safety testing but rather a self-declaration mark from the manufacturer to allow the product’s free movement across Europe. The CE Mark’s aim is to provide a clear indication that a product meets the requirements of relevant CE marking directives and therefore should not be stopped at Member State borders.
Who is responsible?

Under CE Marking, manufacturers are responsible for undertaking a full risk analysis, complying with essential requirements and ensuring that they can provide evidence of having done so. If a harmonized standard applies to the product, the manufacturers have a duty to apply it. An additional duty the manufacturer will also now have is to determine if the standard is fully adequate for the product and its environment, or if the product requires further safety testing before being placed on the open market.

Whilst the vast majority of EU manufacturers are very thorough in ensuring they invest in meeting these standards, there has been criticism that manufacturers from a small number of EU member states have not been so rigorous. This has allowed cheaper, potentially unsafe products to enter the market.

Achieving CE compliance

Reassuringly, market surveillance authorities across the EU are addressing this issue with more active policing of CE Marking. This will ensure a more level playing field for manufacturers across the whole of the EU and will make sure that the CE Mark retains its status as a mark in which trust can be placed.

Achieving CE compliance can be a complex process due to the requirements of individual directives, particularly when combinations of directives apply simultaneously. For the key EU product safety and communications directives, Ege Test Center is able to provide expert help and guidance to support products through the relevant testing process.

For advice on CE Marking a device, please contact us for or

CE Certificate Which Companies Are Required

 CE certificate in our country

By implementing their own standardization polycikas, it eliminates the differences in the requirements of the legislation concerning production in the countries which are involved in the union, and in this way The European Union, which provide the adoption of compliance standards, wants to ensure the same standards for imported products imported from the outside. CE certificate, which is known as CE certificate in our country, represents the production safety and compliance standardization, This means that the product with CE certificate can be used safely and all necessary tests are applied. BTherefore, the provision of these conditions is CE marked, It is important for all companies that produce in our country and want to sell their products to the European Union.

When the consumer buys an equivalent product

CE certificate standards eliminating the differences in the production safety concept from countries’ own production legislation,indexed all the standard differences applied by countries according to the bylaws to a single criterion. With this indexing, no matter what country you are in, When the consumer buys an equivalent product, it can be sure that the product has passed the same test standards for compatibility and use safety.

Even if any company in our country has acquired these permits

Since the products which are produced in countries that do not meet their own standards and which do not have the technical specifications in the legislation determined by the European Union are prevented from entering the union, It is not possible to offer covered products that do not have CE marking in EU countries.Even if any company in our country has acquired these permits, they may have to pass the CE certificate tests to the relevant product at any time after the start of the sale.Re-testing of the product which is being sold at the request of the importer company in the union and If the test results do not meet the required standards, the sale of the company’s product is stopped. You can consult our experienced team in order to bring your production standards to the norms accepted by the European Union and to maintain this standardization so that you do not experience such problems.

CE Certificate for your product

You can mail to to receive CE Certificate for your product or you can click and fill form in page.


Ce Certification

CE Certificate Conformity

Ege Test Center and CE Certification

CE Certificate means compliance with Europa.  There are currently twenty-eight countries in the European Union. CE Certification shows that products sold within these countries are inspected and evaluated for minimum safety, health and environmental protection requirements. Products with CE Certificate have the ability to sell in all of the countries. These products range kitchen robots to cabinets and parquet floors. There are specific criteria for the suitability of each product. The products. CE Certificate products are in our lives most of technological products. For example, the phones and computers that you use are European-based brands, and the products must have a CE certificate for sale in the European Union. CE certificate is a document indicating the quality of the product.

There are some requirements for CE certification conformity assessment. This product is designing and manufacturing product modules. Some modules include only one or two step.  CE certificate conformity assessment modules consist of 8 main categories. All product candidates are subject to internal production control. These;

-AT type examination

– Compliance with type based on internal control of production

– Compliance with the type based on the quality assurance of the production process

– Compliance with type based on internal control of production

– Type-based conformity to product for verification

– Compliance based on unit verification

– Conformity to full quality assurance

Considering these elements, the products of the brand pass through a detailed examination process whether the modules determined by the experts pass the test and inspection stages individually. If the brand is a brand that has CE certificate, the products must be completed and the procedure stage has been completed without the introduction of new products. Brands can easy access this service from the outside. There are companies that carefully examine your products for CE certification. Before contacting this document, you can be sure of your products by contacting these companies to be sure.

CE Certificate for your product

You can mail to to receive CE Certificate for your product or you can click and fill form in page.